Canonical Allele Identifier: CA389475032
Gene: FOXG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.29236893G>C (hg19) chr14:g.28767687G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767687G>C , CM000676.2:g.28767687G>C GRCh38
NC_000014.8:g.29236893G>C , CM000676.1:g.29236893G>C GRCh37
NC_000014.7:g.28306644G>C NCBI36
NG_009367.1:g.5607G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.408G>C ENSP00000516406.1:p.Glu136Asp
ENST00000313071.7:c.408G>C MANE Select ENSP00000339004.3:p.Glu136Asp
ENST00000313071.6:c.408G>C ENSP00000339004.3:p.Glu136Asp
NM_005249.4:c.408G>C NP_005240.3:p.Glu136Asp
NM_005249.5:c.408G>C MANE Select NP_005240.3:p.Glu136Asp
Search 100 bp 5'
Search 100 bp 3'